CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 10 enrolled
Drug / intervention
Clazakizumabdrug
Likely dose
Clazakizumab 25 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03380377
NCT03380377Phase 2Completed

A Phase I/II Trial to Evaluate the Safety and Tolerability of Clazakizumab (Anti-IL-6 Monoclonal) As an Agent to Eliminate Donor Specific HLA Antibodies and Improve Outcomes of Patients With Chronic & Active Antibody-Mediated Rejection Post-Kidney Transplantation

Stanley Jordan, MD·interventional·Posted Dec 21, 2017·Updated May 6, 2025

In Brief

A Phase 2 clinical trial evaluating Clazakizumab for Antibody-mediated Rejection and 5 related conditions. Completed, enrolled 10 participants across 1 site.

Detailed Summary

Antibody mediated rejection (ABMR) is a unique, significant and often severe form of allograft rejection. This single center, phase I/II, open label single-arm exploratory study focuses on enrolling ten patients with biopsy proven chronic antibody medicated rejection and/or donor specific antibody present at time of biopsy. Patients who qualify will be receiving clazakizumab (anti-IL6 monoclonal antibody) monthly x six doses. A protocol biopsy will be performed at 6 months and if improvement is seen, patients will continue another six doses for up to 12 months. For those completing 12 doses, there will be a 12 month protocol biopsy. For those who only received six doses, the next and last study visit will be at 12 months from enrollment. Total study duration is 12 months.

Study Details

Timeline

Phase 2CompletedFinished
201820192020202120222023202420252026
First PostedDec 21, 2017
Enrollment StartFeb 21, 2018
Primary CompletionApr 16, 2024
TodayJul 2, 2026
Enrollment to primary: 6.2 yearsPosted 8.5 years ago

Interventions

Clazakizumabdrug

Clazakizumab 25 mg subcutaneous monthly x 6 doses (or max of 12 doses) will be given to patients who are enrolled in this clinical trial.